Preparation method of cyclohexylamine
A technology of cyclohexylamine and catalyst, which is applied in the field of preparation of chemical product cyclohexylamine, can solve the problems of high cost and environmental pollution, and achieve the effects of long life, high yield and simple preparation process
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Embodiment 1
[0009] Choose γ-Al with an average pore size of 6-8nm and a diameter of φ3mm 2 o 3 30 grams were dried and dehydrated at 250°C for 5 hours, and put into a beaker as a carrier skeleton. Weigh 8 grams of Mg(NO 3 ) 2 ·6H 2 O and 6.9 g Al(NO 3 ) 3 9H 2 O, add 34 grams of distilled water to prepare a mixed solution, pour this solution into the γ-Al 2 o 3 In a beaker, equal-volume impregnation was performed twice. Then dry at 120°C for 6 hours, bake at 1000°C for 6 hours, and cool to obtain a magnesium-aluminum spinel carrier; weigh 1.5 grams of NaHCO 3 Make 10ml solution, impregnate the carrier and dry at 120°C for 6 hours; then weigh 0.25g of PdCl 2 , add 10ml of 10% dilute hydrochloric acid to dissolve, after dissolving, impregnate with equal volume twice with the carrier prepared above, wash with distilled water until there is no chloride ion and sodium ion, then dry at 120°C for 6 hours, and then dry at 500°C Lower roasting for 8 hours.
[0010] The prepared catalys...
Embodiment 2
[0012] Catalyst preparation process is the same as embodiment 1, and the loaded palladium amount of catalyzer changes 0.2% (weight), MgO: Al 2 o 3 =1:4, MgO+Al 2 o 3 The total impregnation amount of is 10%; The phenol feed rate is 2.5 grams / hour, and other reaction conditions are constant, and the transformation rate of phenol is 94.1%, and the selectivity of cyclohexylamine is 74.5%, and the selectivity of dicyclohexylamine is 13.6%.
Embodiment 3
[0014] Choose γ-Al with an average pore size of 12.7nm 2 o 3 As the catalyst carrier skeleton, the catalyst preparation process and preparation conditions are the same as in Example 1, and the reaction conditions are also the same as in Example 1. The conversion rate of phenol is 93.1%, the selectivity of cyclohexylamine is 76.5%, and the selectivity of dicyclohexylamine is 14.7%.
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